Baban A - Search Results

1

Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children.

Baban A, Lodato V, Parlapiano G, di Mambro C, Adorisio R, Bertini ES, Dionisi-Vici C, Drago F, Martinelli D. Baban A, et al. Biomolecules. 2021 Oct 25;11(11):1578. doi: 10.3390/biom11111578. Biomolecules. 2021. PMID: 34827576 Free PMC article. Review.

2

Heterotaxy syndrome with and without spleen: Different infection risk and management.

Piano Mortari E, Baban A, Cantarutti N, Bocci C, Adorisio R, Carsetti R. Piano Mortari E, et al. Among authors: baban a. J Allergy Clin Immunol. 2017 Jun;139(6):1981-1984.e1. doi: 10.1016/j.jaci.2016.10.014. Epub 2016 Nov 15. J Allergy Clin Immunol. 2017. PMID: 27864025 Free article. No abstract available.

3

Clinical Presentation and Natural History of Hypertrophic Cardiomyopathy in RASopathies.

Calcagni G, Adorisio R, Martinelli S, Grutter G, Baban A, Versacci P, Digilio MC, Drago F, Gelb BD, Tartaglia M, Marino B. Calcagni G, et al. Among authors: baban a. Heart Fail Clin. 2018 Apr;14(2):225-235. doi: 10.1016/j.hfc.2017.12.005. Heart Fail Clin. 2018. PMID: 29525650 Review.

4

Bradyarrhythmias in Repaired Atrioventricular Septal Defects: Single-Center Experience Based on 34 Years of Follow-Up of 522 Patients.

Di Mambro C, Calvieri C, Silvetti MS, Tamburri I, Giannico S, Baban A, Albanese S, Brancaccio G, Carotti A, Iorio FS, Drago F. Di Mambro C, et al. Among authors: baban a. Pediatr Cardiol. 2018 Dec;39(8):1590-1597. doi: 10.1007/s00246-018-1934-4. Epub 2018 Jun 13. Pediatr Cardiol. 2018. PMID: 29948031

5

Long-term survival and phenotypic spectrum in heterotaxy syndrome: A 25-year follow-up experience.

Baban A, Cantarutti N, Adorisio R, Lombardi R, Calcagni G, Piano Mortari E, Dallapiccola B, Marino B, Iorio FS, Carsetti R, Digilio MC, Giannico S, Drago F, Carotti A. Baban A, et al. Int J Cardiol. 2018 Oct 1;268:100-105. doi: 10.1016/j.ijcard.2018.02.050. Int J Cardiol. 2018. PMID: 30041775

6

First evidence of maternally inherited mosaicism in TGFBR1 and subtle primary myocardial changes in Loeys-Dietz syndrome: a case report.

Baban A, Magliozzi M, Loeys B, Adorisio R, Alesi V, Secinaro A, Corica B, Vricella L, Dietz HC, Drago F, Novelli A, Amodeo A. Baban A, et al. BMC Med Genet. 2018 Sep 15;19(1):170. doi: 10.1186/s12881-018-0661-2. BMC Med Genet. 2018. PMID: 30219046 Free PMC article.

7

LTBP2-related "Marfan-like" phenotype in two Roma/Gypsy subjects with the LTBP2 homozygous p.R299X variant.

Morlino S, Alesi V, Calì F, Lepri FR, Secinaro A, Grammatico P, Novelli A, Drago F, Castori M, Baban A. Morlino S, et al. Among authors: baban a. Am J Med Genet A. 2019 Jan;179(1):104-112. doi: 10.1002/ajmg.a.10. Epub 2018 Dec 18. Am J Med Genet A. 2019. PMID: 30565850

8

Heart rate reduction strategy using ivabradine in end-stage Duchenne cardiomyopathy.

Adorisio R, Calvieri C, Cantarutti N, D'Amico A, Catteruccia M, Bertini E, Baban A, Filippelli S, Perri G, Amodeo A, Drago F. Adorisio R, et al. Among authors: baban a. Int J Cardiol. 2019 Apr 1;280:99-103. doi: 10.1016/j.ijcard.2019.01.052. Epub 2019 Jan 17. Int J Cardiol. 2019. PMID: 30686494

9

Left pulmonary artery in 22q11.2 deletion syndrome. Echocardiographic evaluation in patients without cardiac defects and role of Tbx1 in mice.

Mastromoro G, Calcagni G, Versacci P, Putotto C, Chinali M, Lambiase C, Unolt M, Pelliccione E, Anaclerio S, Caprio C, Cioffi S, Bilio M, Baban A, Drago F, Digilio MC, Marino B, Baldini A. Mastromoro G, et al. Among authors: baban a. PLoS One. 2019 Apr 1;14(4):e0211170. doi: 10.1371/journal.pone.0211170. eCollection 2019. PLoS One. 2019. PMID: 30933971 Free PMC article.

10

Palmoplantar Keratoderma and Woolly Hair Revealing Asymptomatic Arrhythmogenic Cardiomyopathy.

Guerra L, Magliozzi M, Baban A, Di Mambro C, Di Zenzo G, Novelli A, El Hachem M, Zambruno G, Castiglia D. Guerra L, et al. Among authors: baban a. Acta Derm Venereol. 2019 Jul 1;99(9):831-832. doi: 10.2340/00015555-3216. Acta Derm Venereol. 2019. PMID: 31073624 Free article. No abstract available.

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